SCHMITTERITE-A NEW URANYL TELLURITE from MOCTEZUMA, SONORA Rrcnano V
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
A Review of the Structural Architecture of Tellurium Oxycompounds
Mineralogical Magazine, May 2016, Vol. 80(3), pp. 415–545 REVIEW OPEN ACCESS A review of the structural architecture of tellurium oxycompounds 1 2,* 3 A. G. CHRISTY ,S.J.MILLS AND A. R. KAMPF 1 Research School of Earth Sciences and Department of Applied Mathematics, Research School of Physics and Engineering, Australian National University, Canberra, ACT 2601, Australia 2 Geosciences, Museum Victoria, GPO Box 666, Melbourne, Victoria 3001, Australia 3 Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 Exposition Boulevard, Los Angeles, CA 90007, USA [Received 24 November 2015; Accepted 23 February 2016; Associate Editor: Mark Welch] ABSTRACT Relative to its extremely low abundance in the Earth’s crust, tellurium is the most mineralogically diverse chemical element, with over 160 mineral species known that contain essential Te, many of them with unique crystal structures. We review the crystal structures of 703 tellurium oxysalts for which good refinements exist, including 55 that are known to occur as minerals. The dataset is restricted to compounds where oxygen is the only ligand that is strongly bound to Te, but most of the Periodic Table is represented in the compounds that are reviewed. The dataset contains 375 structures that contain only Te4+ cations and 302 with only Te6+, with 26 of the compounds containing Te in both valence states. Te6+ was almost exclusively in rather regular octahedral coordination by oxygen ligands, with only two instances each of 4- and 5-coordination. Conversely, the lone-pair cation Te4+ displayed irregular coordination, with a broad range of coordination numbers and bond distances. -
New Mineral Names*
American Mineralogist, Volume 85, pages 1321–1325, 2000 NEW MINERAL NAMES* JOHN L. JAMBOR1, NIKOLAI N. PERTSEV2, AND ANDREW C. ROBERTS3 1Department of Earth and Ocean Sciences, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada 2IGREM RAN, Russian Academy of Sciences, Moscow 10917, Staromonetnii 35, Russia 3Geological Survey of Canada, 601 Booth Street, Ottawa K1A 0E8, Canada Andyrobertsite*, calcioandyrobertsite* Bleasdaleite* M.A. Cooper, F.C. Hawthorne, W.W. Pinch, J.D. Grice (1999) W.D. Birch, A. Pring, U. Kolitsch (1999) Bleasdaleite, 3+ Andyrobertsite and calcioandyrobertsite: two new minerals (Ca,Fe )2Cu5(Bi,Cu)(PO4)4(H2O,OH,Cl)13, a new mineral from from the Tsumeb mine, Tsumeb, Namibia. Mineral. Record, Lake Boga, Victoria, Australia. Austral. J. Mineral., 5, 69–75. 30, 181–186. The mineral occurs as tabular crystals, up to 20 µm across The minerals form a lamellar intergrowth that is crystallo- and <1 µm thick, that form dark brown scaly crusts and hemi- graphically continuous. Electron microprobe analyses for spheres up to 100 µm across. Electron microprobe analysis gave andyrobertsite and calcioandyrobertsite gave, respectively, K2O CaO 7.59, CuO 34.79, Bi2O3 15.53, Fe2O3 3.04, Al2O3 0.13, 4.00, 4.05, CaO 1.36, 3.52, MnO 0.64, 0.86, CdO 6.48, 1.26, P2O5 21.70, As2O5 0.34, Cl 1.01, H2O (by difference) ZnO 0.19, 0.04, CuO 31.72, 32.86, As2O5 47.58, 49.56, H2O 16.10, O ≡ Cl 0.23, sum 100 wt%, corresponding to 3+ (calc.) 4.44, 4.61, sum 96.41, 96.75 wt%, corresponding to (Ca1.63Fe 0.46)Σ2.09Cu5(Bi0.80Cu0.25) Σ1.05[(PO4) 3.67(AsO4) 0.04] K1.03(Cd0.61Ca0.30Mn0.11)Σ1.02(Cu4.85Zn0.03)Σ4.88(AsO4)4.04[As(OH)2O2] Σ3.71[Cl0.34(OH)6.15]·7.7H2O. -
The Crystal Structure of Khinite and Polytypism in Khinite and Parakhinite
Mineralogical Magazine, June 2008, Vol. 72(3), pp. 763–770 The crystal structure of khinite and polytypism in khinite and parakhinite 1 1, 2 M. A. COOPER ,F.C.HAWTHORNE * AND M. E. BACK 1 Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba, Canada, R3T 2N2 2 Department of Earth Sciences, Royal Ontario Museum, 100 Queen’s Park, Toronto, Ontario, Canada, M5S 2C6 [Received 2 May 2008; Accepted 17 September 2008] ABSTRACT 2+ 2+ 6+ The crystal structure of khinite, Pb Cu3 Te O6(OH)2, orthorhombic, a = 5.7491(10), b= ˚ ˚ 3 3 10.0176(14), c = 24.022(3) A, V = 1383.6(4) A , space group Fdd2, Z =8,Dcalc = 6.29 g/cm , from the Empire mine, Tombstone, Arizona, USA, has been solved by direct methods and refined to R1 = 3.2% on the basis of 636 unique observed reflections. There is one distinct Te site occupied by Te and coordinated by six O atoms in an octahedral arrangement with a <TeÀO> distance of 1.962 A˚ , typical of Te6+. There are three octahedrally-coordinated Cu sites, each of which is occupied by Cu2+ with <CuÀO> distances of 2.132, 2.151 and 2.308 A˚ , respectively. Each Cu octahedron shows four short meridional bonds (~1.95 A˚ ) and two longapical bonds (2.46 À2.99 A˚ ) characteristic of Jahn- Teller-distorted Cu2+ octahedra. There is one distinct Pb site occupied by Pb and coordinated by six O ˚ atoms and two (OH) groups with a <PbÀO, OH> distance of 2.690 A.TeF6 and CuF6 octahedra share edges and corners to form an [MF2] (where F = O, OH) layer of composition [TeCu3F8]. -
CLIFFORDITE-A NEW TELLURITE MINERAL from MOCTEZUMA, SONORA, MEXICO Rrcnanp V. G,Trnns, Kazerccki Berylco Indwstries, Inc', Boyer
THE AMERICAN MINERALOGIST' VOL .54, MAY'JUNE, I969 CLIFFORDITE-A NEW TELLURITE MINERAL FROM MOCTEZUMA,SONORA, MEXICO Rrcnanp V. G,trNns,Kazerccki Berylco Indwstries, Inc', BoYertown,P ennsYlaani'a19 5 1 2. ABsrRAcr This new mineral occurs along joint surfaces in the oxidized zone of the san Miguel mine, a telluriurn-gold-silver prospect near Moctezuma, sonora, associated with mackayite, barite, quartz, and limonite. It has also been found in very small quantities at the Mocte- zuma mine in the same district, associated with native tellurium and paratellurite in small vugs. The small octahedrons are bright yellow with adamantine luster. The mineral is iso- gave 31.3 percent U and 52.6 percent Te, which corresponds closely to the formula uTeroa. Specific gravity, measured on synthetic material, was 6.57, and calculated specific gravity ls o./o. Singlecrystalprecessionphotographsshowedo:11.371Aandspacegroup Pa3,Z:8' The principal powder lines with corresponding intensities are 3.273 (10): 2.844 (8): 2.007 (8): 2.755(7): and r.712(7). Cliffordite from the Moctezuma mine contains a little lead and is identical with the sup- posed lead oxy-fluoride from this mine described by Mandarino and Williams in 1961. The lead oxy-fluoride is therefore not a valid species. The name is for Clifiord Frondel, in recognition of his many contributions to the study of the mineralogy of uranium. INtnooucuow In 1963 the writer noticed crusts of bright yellow microscopic crystals on some mackayite specimensfrom the San Miguel Mine, Moctezuma, Sonora,Mexico. Subsequentinvestigations establishedthat thesecrystals consistedof uranium tellurite, a new mineral. Later on it was found that this mineral is identical with a substance from the Moctezuma Mine which had been first observedin 1961 and mistakenly identified as lead oxy-fluoride. -
Lead-Tellurium Oxysalts from Otto Mountain Near Baker, California: Part VI. Telluroperite, Pb3teo4cl2, the Te Analog of Perite A
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Caltech Authors American Mineralogist, Volume 95, pages 1569–1573, 2010 Lead-tellurium oxysalts from Otto Mountain near Baker, California: VI. Telluroperite, 4+ Pb3Te O4Cl2, the Te analog of perite and nadorite ANTHONY R. KA MPF ,1,* STU AR T J. MILL S ,2 ROBE R T M. HOU S LEY,3 JO S EPH MAR TY,4 A ND BR ENT THO R NE 5 1Mineral Sciences Department, Natural History Museum of Los Angeles County, 900 Exposition Blvd., Los Angeles, California 90007, U.S.A. 2Department of Earth and Ocean Sciences, University of British Columbia, Vancouver, British Columbia V6T 1Z4, Canada 3Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, California 91125, U.S.A. 43457 E. Silver Oak Road, Salt Lake City, Utah 84108, U.S.A. 53898 S. Newport Circle, Bountiful, Utah 84010, U.S.A. AB S T RA CT 4+ Telluroperite, Pb3Te O4Cl2, is a new tellurite from Otto Mountain near Baker, California. The new mineral occurs on fracture surfaces and in small vugs in brecciated quartz veins in direct association with acanthite, bromine-rich chlorargyrite, caledonite, cerussite, galena, goethite, and linarite. Various other secondary minerals occur in the veins, including six new tellurates, housleyite, markcooperite, paratimroseite, ottoite, thorneite, and timroseite. Telluroperite is orthorhombic, space group Bmmb, a = 5.5649(6), b = 5.5565(6), c = 12.4750(14) Å, V = 386.37(7) Å3, and Z = 2. The new mineral occurs as rounded square tablets and flakes up to 0.25 mm on edge and 0.02 mm thick. -
New Mineral Names*,†
American Mineralogist, Volume 102, pages 2525–2531, 2017 New Mineral Names*,† FERNANDO CÁMARA1, DMITRIY I. BELAKOVSKIY2, YULIA UVAROVA3, AND OLIVIER C. GAGNE4 1Dipartimento di Scienze della Terra “Ardito Desio”, Universitá di degli Studi di Milano, Via Mangiagalli, 34, 20133 Milano, Italy 2Fersman Mineralogical Museum, Russian Academy of Sciences, Leninskiy Prospekt 18 korp. 2, Moscow 119071, Russia 3CSIRO Mineral Resources, CSIRO, ARRC, 26 Dick Perry Avenue, Kensington, Western Australia 6151, Australia 4Department of Geological Sciences, University of Manitoba, Winnipeg, Manitoba R3T 2N2, Canada IN THIS ISSUE This New Mineral Names has entries for 14 new minerals, including ferricoronadite, garronite-Na, gauthierite, gurimite, hansesmarkite, hexacelsian, hydroxylgugiaite, hydropascoite, meierite, parascandolaite, petersite-(Ce), rietveldite, rossovskyite, and telluromandarinoite. 3+ 4+ FERRICORONADITE* based on 8 cations pfu (and Mn /Mn from charge balance) is Pb1.03 4+ 3+ 3+ N.V. Chukanov, S.M. Aksenov, S. Jančev, I.V. Pekov, J. Göttlicher, Y.S. Ba0.32(Mn4.85Fe1.35Mn1.18Ti0.49Al0.09Zn0.04)Σ8.00O16. The strongest lines in the Polekhovsky, V.S. Rusakov, Y.V. Nelyubina, and K.V. Van (2016) A X-ray powder diffraction pattern are [d Å (I%; hkl)]: 3.497 (33; 220), 4+ 3+ 3+ 3.128 (100; 130,130), 2.424 (27; 121,121), 2.214 (23; 240,240), 2.178 new mineral species ferricoronadite, Pb[Mn6 (Fe ,Mn )2]O16: min- eralogical characterization, crystal chemistry and physical properties. (17; 031), 1.850 (15; 141,141), 1.651 (16; 060), 1.554 (18; 251,251). The Physics and Chemistry of Minerals, 43, 503–514. unit-cell parameters refined from the powder data are: a = 9.9073(9), c = 2.9023(4) Å, V = 284.87 Å3. -
THE CRYSTAL STRUCTURE of WINSTANLEYITE, Tite3o8, from the GRAND CENTRAL MINE, TOMBSTONE, ARIZONA
1469 The Canadian Mineralogist Vol. 41, pp. 1469-1473 (2003) THE CRYSTAL STRUCTURE OF WINSTANLEYITE, TiTe3O8, FROM THE GRAND CENTRAL MINE, TOMBSTONE, ARIZONA LUCA BINDI§ AND CURZIO CIPRIANI Museo di Storia Naturale – sez. di Mineralogia e Litologia – Università degli Studi di Firenze, via La Pira 4, I–50121 Firenze, Italy ABSTRACT We have refined the crystal structure of winstanleyite from the type locality, the Grand Central mine, Tombstone, Arizona, in 3 space group I21/a¯3 to a final R index of 2.03%. Unit-cell parameters of the crystal examined are: a 10.965(1) Å, V 1318.3(2) Å , Z = 8. The structure previously reported for the synthetic analogue was confirmed, although a higher precision of refinement was achieved. The crystal-chemical environment of both Ti and Te cations is considered in relation with that in other tellurite struc- tures. Keywords: winstanleyite, walfordite, crystal-structure refinement, Tombstone, Arizona. SOMMAIRE Nous avons affiné la structure cristalline de la winstanleyite provenant de la localité type, la mine Grand Central, à Tomb- stone, en Arizona, dans le groupe spatial I21/a¯3 jusqu’à un résidu final R de 2.03%. Les paramètres réticulaire du cristal choisi sont: a 10.965(1) Å, V 1318.3(2) Å3, Z = 8. Nous confirmons la structure décrite antérieurement pour l’analogue synthétique, avec une précision améliorée. Nous évaluons l’environnement cristallochimique des cations Ti et Te en relation de celui d’autres structures de tellurites. (Traduit par la Rédaction) Mots-clés: winstanleyite, walfordite, affinement de la structure, Tombstone, Arizona. 4+ 4+ INTRODUCTION of the synthetic phase M Te 3O8 (Meunier & Galy 1971), and classified the mineral as the Fe3+ analogue The compound TiTe3O8 was first synthesized by of winstanleyite. -
Table S1. Tellurium Minerals: Number of Species-Defining’S Elements (N) Chemical Formula, and Number of Localities (NL)
Table S1. Tellurium minerals: Number of species-defining’s elements (N) chemical formula, and number of localities (NL). N Mineral Chemical formula NL References 4 Adanite Pb2(TeO3)(SO4) 1 1 6 Agaite Pb3[Cu(TeO5OH)](CO3)(OH) 2 2 4 Alburnite Ag8GeTe2S4 1 3 4 Aleksite PbBi2Te2S2 28 4 2 Altaite PbTe 489 5 5 Andychristyite PbCu(TeO5)·H2O 1 6 3 Andymcdonaldite Fe2TeO6 1 7 5 Backite Pb2AlTeO6Cl 1 8 6 Bairdite Pb2Cu4Te2O10(OH)2(SO4)·H2O 4 9 3 Baksanite Bi6Te2S3 4 10 3 Balyakinite Cu(TeO3) 4 11 5 Benleonardite Ag15CuSb2S7Te4 20 12 3 Bezsmertnovite Au4CuTe 6 13 4 Bilibinskite PbAu3Cu2Te2 12 14 4 Bodieite Bi2(TeO3)2(SO4) 4 15 3 Borovskite Pd3SbTe4 11 16 4 Brumadoite Cu3(TeO4)(OH)4·5HO 1 17 5 Buckhornite Pb2AuBiTe2S3 13 18 6 Burckhardtite Pb2(Fe3+Te6+)Σ2(AlSi3O8)O6 4 19 2 Calaverite AuTe2 361 20 2 Cameronite Cu5Cu3Te10 1 21 3 Carlfriesite CaTe6+(Te4+)2O8 4 22 3 Cervelleite Ag4TeS 42 23 4 Cesbronite Cu3Te6+O4(OH)4 3 24 3 Chekhovichite Bi2Te4O11 5 25 4 Chenguodaite Ag9FeTe2S4 2 26 5 Cheremnykhite Pb3Zn3(TeO6)(VO4)2 1 27 4 Chiluite Bi6Te2Mo6+2O21 1 28 7 Choloalite Pb3(Cu2Sb)Σ3Te6O18Cl 7 29 5 Chromschieffelinite Pb10[Te2O8(OH)3]2(TeO2(OH)4)2(CrO4)·5H2O 1 30 3 Cliffordite UTe3O9 4 31 2 Coloradoite HgTe 169 32 4 Cuzticite Fe2(TeO6)·3H2O 2 33 3 Dagenaisite Zn3(TeO6) 1 34 5 Debattistiite Ag18HgAs12S24Te4 1 35 4 Denningite CaMnTe4O10 2 36 5 Dugganite Pb3Zn3(TeO6)(AsO4)2 18 37 5 Eckhardite CaCu(TeO5) H2O 3 38 2 4 Emmonsite Fe2(TeO3)3·2H2O 34 39 2 Empressite AgTe 43 40 7 Eurekadumpite Cu16(TeO3)2(AsO4)3Cl(OH)18·7H2O 5 41 5 Eztlite Pb2Fe3(TeO3)3(SO4)O2Cl 2